510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K231539Substantially Equivalent

pRESET LITE Thrombectomy Device

Phenox Inc, Galway, IE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K231539 is the FDA 510(k) clearance record for pRESET LITE Thrombectomy Device, a class II device, cleared for Phenox Limited on under FDA product code POL (Neurovascular Mechanical Thrombectomy Device For Acute Ischemic Stroke Treatment). FDA's definition for product code POL reads: "A neurovascular mechanical thrombectomy device for acute ischemic stroke treatment is a prescription device used in the treatment of acute ischemic stroke to improve clinical outcomes. The device is delivered into the neurovasculature with...". FDA records list 7 510(k) clearances for Phenox Limited, from to . As of , FDA records show no recalls naming K231539.

Clearance record

Decision date
Received
(144 days to decision)
Product code
POL Neurovascular Mechanical Thrombectomy Device For Acute Ischemic Stroke Treatment
Regulation
21 CFR 882.5600
Device class
Class II
Review panel
Neurology
Applicant
Phenox Limited Kamrick Ct., Galway, IE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code POL

Trailing 12 months

FDA records hold no clearances under product code POL in the trailing twelve months.

FDA records show no clearances under product code POL in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code POL, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260